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PMID: 3865712 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Intermolecular exon ligation of the rRNA precursor of Tetrahymena: oligonucleotides can function as 5' exons.

Cell ·Vol. 43 ·No. 2 Pt 1 ·1985-12-00 ·Pages 431-7

Inoue T, Sullivan FX, Cech TR

Abstract

The dinucleotide CpUOH, when incubated with self-splicing Tetrahymena pre-rRNA in the absence of GTP, functions as a 5' exon. It cleaves the precursor exactly at the 3' splice site and becomes covalently ligated to the 3' exon. Other oligonucleotides with sequences that resemble CUCUCU, the sequence at the 3' end of the 5' exon, can add to the 3' exon in this reaction. Such splicing in trans is most readily explained by a site within the intervening sequence that binds the last few nucleotides of the 5' exon. This binding site functions in splice site recognition and is also part of the active site of the ribozyme. The mechanism by which 5' splice sites are selected in Tetrahymena rRNA and group I mitochondrial RNA splicing is like that used in nuclear mRNA splicing, in that it involves specific pairing of bases adjacent to the splice site with a complementary RNA sequence.

MeSH Terms
Animals Base Sequence Binding Sites Dinucleoside Phosphates Oligonucleotides/metabolism RNA Splicing RNA, Ribosomal/biosynthesis Tetrahymena/metabolism
Chemicals
Dinucleoside Phosphates Oligonucleotides RNA, Ribosomal
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Inoue T
Sullivan F X
Cech T R
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1985-12-00
Pages
431-7
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NIGMS NIH HHS · GM28039 · United States
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